PE20110387A1 - Aminotriazolo-piridinas como inhibidores de cinasa - Google Patents

Aminotriazolo-piridinas como inhibidores de cinasa

Info

Publication number
PE20110387A1
PE20110387A1 PE2011000599A PE2011000599A PE20110387A1 PE 20110387 A1 PE20110387 A1 PE 20110387A1 PE 2011000599 A PE2011000599 A PE 2011000599A PE 2011000599 A PE2011000599 A PE 2011000599A PE 20110387 A1 PE20110387 A1 PE 20110387A1
Authority
PE
Peru
Prior art keywords
pyran
tetrahydro
methyl
triazolo
pyridin
Prior art date
Application number
PE2011000599A
Other languages
English (en)
Spanish (es)
Inventor
Sogole Bahmanyar
R J Bates
Kate Blease
Thomas Oran Daniel
Jan Elsner
Paul Erdman
Bruce Fahr
Gregory Fergunson
Branden Lee
Lisa Nadolny
Garrick Packard
Patrick Papa
Jennifer Riggs
Patricia Rohane
John Sapienza
Victor Sloan
Randall Stevens
Lida Tehrani
Jayashree Tikhe
Eduardo Torres
Brandon Wade Whitefield
Jingjing Zhao
Andrew Antony Calabrese
Mercedes Delgado
Veronique Plantevin-Krenitsky
Yoshitaka Satoh
Andrew Wallace
Sabita Sankar
Original Assignee
Signal Pharm Llc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=41228355&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20110387(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Signal Pharm Llc filed Critical Signal Pharm Llc
Publication of PE20110387A1 publication Critical patent/PE20110387A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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    • A61P7/04—Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
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    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • C07D519/04—Dimeric indole alkaloids, e.g. vincaleucoblastine
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • C07D519/06—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00 containing at least one condensed beta-lactam ring system, provided for by groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00, e.g. a penem or a cepham system

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Diabetes (AREA)
  • Immunology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Neurology (AREA)
  • Hematology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Pulmonology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Rheumatology (AREA)
  • Dermatology (AREA)
  • Oncology (AREA)
  • Obesity (AREA)
  • Communicable Diseases (AREA)
  • Pain & Pain Management (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Endocrinology (AREA)
  • Psychology (AREA)
  • Urology & Nephrology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Emergency Medicine (AREA)
  • Transplantation (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
PE2011000599A 2008-09-08 2009-09-08 Aminotriazolo-piridinas como inhibidores de cinasa PE20110387A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US9521708P 2008-09-08 2008-09-08
US23047909P 2009-07-31 2009-07-31

Publications (1)

Publication Number Publication Date
PE20110387A1 true PE20110387A1 (es) 2011-06-22

Family

ID=41228355

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2011000599A PE20110387A1 (es) 2008-09-08 2009-09-08 Aminotriazolo-piridinas como inhibidores de cinasa

Country Status (22)

Country Link
US (2) US8299056B2 (fr)
EP (1) EP2344494B1 (fr)
JP (1) JP5689060B2 (fr)
KR (1) KR20110053266A (fr)
CN (2) CN102203093B (fr)
AU (1) AU2009288618B2 (fr)
BR (1) BRPI0918854A2 (fr)
CA (1) CA2735806A1 (fr)
CL (1) CL2011000480A1 (fr)
CO (1) CO6531502A2 (fr)
CR (1) CR20110132A (fr)
EC (1) ECSP11010945A (fr)
ES (1) ES2581565T3 (fr)
IL (1) IL211549A (fr)
MX (1) MX2011002536A (fr)
NI (1) NI201100048A (fr)
NZ (1) NZ591551A (fr)
PE (1) PE20110387A1 (fr)
RU (1) RU2552642C2 (fr)
TW (1) TWI453207B (fr)
WO (1) WO2010027500A1 (fr)
ZA (1) ZA201101586B (fr)

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JPS60100852A (ja) * 1984-09-28 1985-06-04 Hitachi Ltd 情報伝送方法
WO2006020049A2 (fr) 2004-07-15 2006-02-23 Amr Technology, Inc. Tetrahydroisoquinolines a substitution aryle et heteroaryle et leur utilisation pour bloquer le recaptage de la norepinephrine, la dopamine et la serotonine
JP5496915B2 (ja) 2008-02-13 2014-05-21 シージーアイ ファーマシューティカルズ，インコーポレーテッド ６−アリール−イミダゾ［１，２−ａ］ピラジン誘導体、その製造方法、及びその使用方法
CA2713716A1 (fr) 2008-02-22 2009-08-27 F. Hoffmann-La Roche Ag Modulateurs de la beta-amyloide
US9156812B2 (en) 2008-06-04 2015-10-13 Bristol-Myers Squibb Company Crystalline form of 6-[(4S)-2-methyl-4-(2-naphthyl)-1,2,3,4-tetrahydroisoquinolin-7-yl]pyridazin-3-amine
BRPI0909945A2 (pt) * 2008-06-20 2015-07-28 Genentech Inc "composto, composição farmacêutica, método para tratar ou atenuar a gravidade de uma doença ou condição responsiva à inibição da atividade jak2 quinase em um paciente, kit para o tratamento de uma doença ou distúrbio responsivo à inibição da jak quinase"
GB0817207D0 (en) 2008-09-19 2008-10-29 Pimco 2664 Ltd therapeutic apsac compounds and their use
WO2010040661A1 (fr) 2008-10-09 2010-04-15 F. Hoffmann-La Roche Ag Modulateurs pour l'amyloïde bêta
EP2355817A1 (fr) 2008-11-10 2011-08-17 F. Hoffmann-La Roche AG Modulateurs de la gamma secrétase hétérocyclique
PT2373169E (pt) 2008-12-08 2015-10-05 Gilead Connecticut Inc Inibidores de imidazopirazina da syk
MX2011006094A (es) 2008-12-08 2011-11-29 Gilead Connecticut Inc Inhibidores de imidazopirazina syk.
US8450321B2 (en) 2008-12-08 2013-05-28 Gilead Connecticut, Inc. 6-(1H-indazol-6-yl)-N-[4-(morpholin-4-yl)phenyl]imidazo-[1,2-A]pyrazin-8-amine, or a pharmaceutically acceptable salt thereof, as a SYK inhibitor
SG173610A1 (en) * 2009-02-13 2011-09-29 Fovea Pharmaceuticals Sa [1, 2, 4] triazolo [1, 5 -a] pyridines as kinase inhibitors
AU2011211410B2 (en) * 2009-02-13 2013-01-31 Fovea Pharmaceuticals Sa [1,2,4] triazolo [1,5-A] pyridines as kinase inhibitors
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EP2344494B1 (fr) 2016-04-20
US20130005707A1 (en) 2013-01-03
CL2011000480A1 (es) 2011-09-16
US8299056B2 (en) 2012-10-30
JP5689060B2 (ja) 2015-03-25
KR20110053266A (ko) 2011-05-19
AU2009288618A1 (en) 2010-03-11
AU2009288618B2 (en) 2014-10-02
BRPI0918854A2 (pt) 2019-02-26
CN102203093A (zh) 2011-09-28
CR20110132A (es) 2011-06-20
CO6531502A2 (es) 2012-09-28
CN102203093B (zh) 2015-05-13
RU2552642C2 (ru) 2015-06-10
CN104910148B (zh) 2017-06-27
IL211549A0 (en) 2011-05-31
IL211549A (en) 2017-04-30
WO2010027500A1 (fr) 2010-03-11
NI201100048A (es) 2011-11-17
TW201024293A (en) 2010-07-01
EP2344494A1 (fr) 2011-07-20
CN104910148A (zh) 2015-09-16
ZA201101586B (en) 2012-05-30
NZ591551A (en) 2011-10-28
US20100093698A1 (en) 2010-04-15
ES2581565T3 (es) 2016-09-06
MX2011002536A (es) 2011-04-04
ECSP11010945A (es) 2011-05-31
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JP2012502029A (ja) 2012-01-26
CA2735806A1 (fr) 2010-03-11

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